Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
  • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
  • C07D487/04—Ortho-condensed systems
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P11/00—Drugs for disorders of the respiratory system
  • A61P11/08—Bronchodilators

Definitions

• the present invention relates to tetrahydrotriazolo[3,4-a]phthalazines having a (cyclic amino)alkylamino substituent at the 6-position. More particularly, it relates to compounds having the following general formula ##STR1## wherein R is hydrogen or lower alkyl of 1-4 carbon atoms; Alk is alkylene of 2-4 carbon atoms; m is 0 or 1; and n is 4 or 5; and the pharmaceutically acceptable acid addition salts thereof.
• the lower alkyl group referred to above can be exemplified by groups such as methyl, ethyl, propyl and butyl.
• the alkylene groups referred to above separate the nitrogens attached thereto by at least two carbon atoms and can be exemplified by ethylene, propylene, trimethylene or tetramethylene.
• the cyclic amino group contains only carbon and one nitrogen and the cyclic amines involved are 1-pyrrolidinyl or 1-piperidinyl, both optionally substituted with a methyl group.
• Preferred compounds of the present invention are those wherein Alk is ethylene.
• a further preferred embodiment are those compounds wherein Alk is ethylene and R is hydrogen.
• Acid addition salts of the amines of the present invention with pharmaceutically acceptable acids are equivalent to the amines for the purposes of this invention.
• Illustrative of such salts are the salts with inorganic acids such as, for example, hydrochloric, hydrobromic, sulfuric, phosphoric and like acids; with organic carboxylic acids such as, for example, acetic, propionic, glycolic, lactic, pyruvic, malonic, succinic, fumaric, malic, tartaric, citric, ascorbic, maleic, hydroxymaleic and dihydroxymaleic, benzoic, phenylacetic, 4-aminobenzoic, 4-hydroxybenzoic, anthranilic, cinnamic, salicylic, 4-aminosalicylic, 2-phenoxybenzoic, 2-acetoxybenzoic, mandelic and like acids; and with organic sulfonic acids such as methanesulfonic acid and p-toluenesulfonic acid.
• the substituted tetrahydrotriazolo[3,4-a]phthalazine compounds as described above are bronchodilators and are thus useful for the treatment of bronchial disorders such as bronchial asthma.
• the present invention is further directed to a method of effecting bronchodilation.
• an effective bronchodilating amount of 1 or more substituted tetrahydrotriazolo[3,4-a]phthalazines of this invention is administered internally to a mammal in need thereof by a route effective to bring the compound into contact with the bronchial and tracheal tissues of the mammal.
• Administration can be carried out either by a parenteral route, such as by intravenous, intraperitoneal or intramuscular injection, or by introduction into the gastrointestinal tract via oral or rectal administration, for example, in order to bring about such contact via the blood stream, or by intratracheal administration, by inhalation of a solution in the form of a spray or by inhalation of an aerosol formulation.
• the effective bronchodilating amount of the compound that is, the amount sufficient to inhibit or alleviate bronchial spasm, depends on various factors such as the size, type and age of the animal to be treated, the particular compound or pharmacologically-acceptable salt employed, the route and frequency of administration, the severity of any spasm and the causative agent involved, and the time of administration.
• the dosage to be administered can be ascertained by conventional range finding techniques, for example, by observing the bronchodilator activity produced at different dosage rates.
• the compounds can be administered at dosage rates ranging from about 1 to about 200 milligrams of substituted tetrahydrotriazolo[3,4-a]phthalazine compound per kilogram of animal body weight with other ranges being from about 1 to about 100 or from 1 to about 50 milligrams per kilogram. It is generally desirable to administer individual dosages at the lowest amount which provides the desired protection from bronchial spasm consonant with a convenient dosing schedule. Dosage units adaptable to oral administration such as tablets, capsules, lozenges, elixirs, syrups and the like are generally preferred and the active compound can be formulated in conventional time release capsule or tablet formulations although injectable compositions or sprays and aerosols for inhalation are preferred when rapid action is desired.
• the active ingredient is preferably incorporated in a composition comprising a pharmaceutical carrier and from about 5 to about 90 percent by weight of the substituted tetrahydrotriazolo[3,4-a]phthalazine compound or a pharmaceutically-acceptable salt thereof.
• pharmaceutical carrier refers to known pharmaceutical excipients useful in formulating pharmaceutically active compounds for internal administration to animals, and which are substantially non-toxic and non-sensitizing under conditions of use.
• compositions can be prepared by known techniques for the preparation of tablets, capsules, lozenges, troches, suppositories, elixirs, syrups, emulsions, dispersions, wettable and effervescent powders, sterile injectable compositions and solutions for sprays, and can contain suitable excipients known to be useful in the preparation of the particular type of composition desired.
• suitable pharmaceutical carriers and formulation techniques are found in standard texts, such as Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, Pa.
• test compounds were administered to guinea pigs either orally or by intraperitoneal injection and the guinea pigs were challenged by exposure to a histamine aerosol, generally 1 hour later although several time periods can be used. Untreated animals collapsed when exposed to the histamine aerosol. In these operations, the animals were observed and collapse times were recorded. The collapse times observed were then compared statistically with control animals treated with water alone with the control group usually being a long-term cumulative control. When tested by the above procedure, the compounds of the present invention were found to produce a bronchodilating effect.
• the compounds of the present invention are conveniently prepared by the reaction of a 6-halo-7,8,9,10-tetrahydro-1,2,4-triazolo[3,4-a]phthalazine with an appropriate amine of the formula ##STR2## where Alk, m and n are defined as above.
• the 6-halo substituent is preferably chlorine although it can also be bromine.
• This 6-halo compound is reacted with an excess of the amine in an inert solvent medium. More specifically, the reaction is carried out at the boiling temperature under reflux.
• the solvent medium can actually be an excess of the amine used in the reaction or an inert organic solvent such as 2-methoxyethanol.
• the product is recovered by conventional procedures such as concentration under reduced pressure or by pouring the reaction mixture into ice water. The process usually gives the product as the free amine and this can be converted to the acid addition salts by standard procedures, e.g., dissolving the amine in ethanol and adding the anhydrous acid, whereupon the salt precipitates out
• Example 2 The procedure of Example 1 was repeated using 6-chloro-7,8,9,10-tetrahydro-1,2,4-triazolo[3,4-a]phthalazine and the appropriate amine. The product obtained was then reacted with hydrogen chloride according to the procedure described in the first paragraph of Example 2 to give the corresponding salt. In this way, the following compounds were obtained:
• 1-Chloro-4-hydrazino-5,6,7,8-tetrahydrophthalazine also nameable as 3-chloro-4,5-tetramethylene-6-hydrazino pyridazine
• the mixture was heated at the boiling temperature under reflux for 2 hours.
• the mixture was concentrated by evaporation under reduced pressure, and the oily residue mixed with saturated aqueous sodium bicarbonate solution.
• the resulting white solid was separated by filtration, washed with water and dried in air.
• the 6-chloro-7,8,9,10-tetrahydro-1,2,4-triazolo[3,4-a]phthalazine product was recrystallized from alcohol-hexane and found to melt at 124°-125° C.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• Public Health (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Medicinal Chemistry (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Pharmacology & Pharmacy (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• General Health & Medical Sciences (AREA)
• Pulmonology (AREA)
• Veterinary Medicine (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)
• Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
• Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
• Peptides Or Proteins (AREA)
• Preparation Of Compounds By Using Micro-Organisms (AREA)
• Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Priority Applications (17)

Applications Claiming Priority (1)

Publications (1)

Family

ID=23642869

Family Applications (1)

Country Status (17)

Cited By (2)

Families Citing this family (7)

Citations (15)

• 1982
  • 1982-09-07 US US06/414,766 patent/US4487930A/en not_active Expired - Lifetime
• 1983
  • 1983-09-02 JP JP58160604A patent/JPS5965092A/ja active Granted
  • 1983-09-02 GR GR72367A patent/GR78970B/el unknown
  • 1983-09-02 ZA ZA836551A patent/ZA836551B/xx unknown
  • 1983-09-05 AT AT83108711T patent/ATE23339T1/de not_active IP Right Cessation
  • 1983-09-05 NZ NZ205493A patent/NZ205493A/en unknown
  • 1983-09-05 EP EP83108711A patent/EP0104506B1/fr not_active Expired
  • 1983-09-05 DE DE8383108711T patent/DE3367393D1/de not_active Expired
  • 1983-09-05 IL IL69659A patent/IL69659A/xx not_active IP Right Cessation
  • 1983-09-05 AU AU18713/83A patent/AU555725B2/en not_active Ceased
  • 1983-09-05 PH PH29493A patent/PH18334A/en unknown
  • 1983-09-05 ES ES525368A patent/ES525368A0/es active Granted
  • 1983-09-06 CA CA000438466A patent/CA1204753A/fr not_active Expired
  • 1983-09-06 KR KR1019830004193A patent/KR880002685B1/ko not_active IP Right Cessation
  • 1983-09-06 IE IE2096/83A patent/IE55908B1/en not_active IP Right Cessation
  • 1983-09-06 NO NO833181A patent/NO833181L/no unknown
  • 1983-09-06 DK DK404383A patent/DK160310C/da not_active IP Right Cessation

Patent Citations (15)

Non-Patent Citations (8)

Also Published As

Similar Documents

Legal Events